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Dinuclear complexes with ferrocenyl and oxomolybdenum(V) fragments linked by a conjugated spacer have been prepared and studied by spectroelectrochemistry; the first oxidation (ferrocene → ferrocenium) affords spectra characteristic of localized ferrocenium and oxo-Mo(V) fragments, but the second oxidation [Mo(V)→Mo(VI)] results in very intense new transitions in the near-IR region which we ascribe to a fully allowed π → π* transition of the bridging group, which now has quinonoidal character.
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Lee et al. (1998) studied this question.
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